Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014255019

FEI Number

3014255019

Entity Name

MAUSER BENELUX B.V.

City/State/Country

Oosterhout Noord-Brabant, NL

Establishment Address

Souvereinstraat 1, Oosterhout Noord-Brabant 4903RH, NL

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

MAUSER Benelux B.V. (Owner Number: 10056535)

Owner / Operator Contact Address

Souvereinstraat 1, Oosterhout, NL-NB 4903RH, NL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K170513

PMA Number

N/A

All Registered Proprietary Names

MAUSER PGII Sharps Container

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MMK	Container, Sharps	General Hospital	Class 2	880.5570	2017-12-19

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp. Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

MAUSER Benelux B.V.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014255019. Last updated year: 2026. Please use registration number 3014255019 when referencing this establishment in official correspondence.